The DOI matches its Crossref record.
Differential expression of p63 isoforms in normal tissues and neoplastic cells
Abstract
The p63 gene encodes at least six different proteins with homology to the tumour suppressor protein p53 and the related p53 family member p73. So far, there have been limited data concerning the expression patterns of individual p63 proteins, due to a lack of reagents that distinguish between the different isoforms. Three antibodies have been produced specifically directed against the two N‐terminal isoforms (TAp63 and ΔNp63) and the C‐terminal region of the p63α proteins. TAp63 proteins are located suprabasally in stratified epithelia compared with the N‐terminal truncated forms, which are more abundantly expressed in the basal cell layer, indicating a switch in expression of p63 isoforms during normal cellular differentiation. Analysis of squamous cell carcinomas shows ΔNp63α to be the most widely expressed isoform, compatible with a role for this protein in promoting neoplastic cell growth in these tissues. ΔNp63 protein expression is also restricted to basal cells in breast and prostate, whilst TAp63 isoforms are more widely expressed in these tissues as well as in tumours at these sites. TAp63, but not ΔNp63 or p63α, is detected in normal colon and in colon carcinoma. TAp63 proteins are also expressed in the nuclei of a sub‐population of lymphoid cells and in most malignant lymphomas, whereas ΔNp63 proteins are not expressed. Taken together, a hitherto unrecognized regulation of p63 isoform expression in vivo has been uncovered, with different p63 proteins expressed during differentiation and in different cell types. The data indicate roles for specific p63 isoforms not only in maintaining epithelial stem cell populations, but also in cellular differentiation and neoplasia. Copyright © 2002 John Wiley & Sons, Ltd.
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Citations
Cited by
p63 Is Essential for the Proliferative Potential of Stem Cells in Stratified Epithelia
Senoo, M., Pinto, F., Crum, C. P., & McKeon, F. (2007) · Cell · doi:10.1016/j.cell.2007.02.045 · Cited by 881
p63 and p73, the ancestors of p53
Dotsch, V., Bernassola, F., Coutandin, D., Candi, E., & Melino, G. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004887 · Cited by 326
Complex controls: the role of alternative promoters in mammalian genomes
Landry, J.-R., Mager, D. L., & Wilhelm, B. T. (2003) · Trends in Genetics · doi:10.1016/j.tig.2003.09.014 · Cited by 331
Maintaining epithelial stemness with p63
Melino, G., Memmi, E. M., Pelicci, P. G., & Bernassola, F. (2015) · Science Signaling · doi:10.1126/scisignal.aaa1033 · Cited by 139
Shimomura, Y., Wajid, M., Shapiro, L., & Christiano, A. M. (2008) · Development · doi:10.1242/dev.006718 · Cited by 122
Actinic keratosis: a clinical and epidemiological revision
Schmitt, J. V., & Miot, H. A. (2012) · Anais Brasileiros de Dermatologia · doi:10.1590/s0365-05962012000300012 · Cited by 120
Repression of p63 and induction of EMT by mutant Ras in mammary epithelial cells
Yoh, K. E., Regunath, K., Guzman, A., Lee, S.-M., Pfister, N. T., Akanni, O., Kaufman, L. J., Prives, C., & Prywes, R. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1613417113 · Cited by 75
ΔNp63 transcriptionally regulates ATM to control p53 Serine-15 phosphorylation
Craig, A. L., Holcakova, J., Finlan, L. E., Nekulova, M., Hrstka, R., Gueven, N., DiRenzo, J., Smith, G., Hupp, T. R., & Vojtesek, B. (2010) · Molecular Cancer · doi:10.1186/1476-4598-9-195 · Cited by 37
Self-citationNectin‐4 and p63 immunohistochemical expression in canine prostate tumourigenesis
Della Salda, L., Massimini, M., Romanucci, M., Palmieri, C., Perillo, A., Grieco, V., Malatesta, D., Spinillo, M. A., Passantino, G., Dondi, F., et al. (2019) · Veterinary and Comparative Oncology · doi:10.1111/vco.12469 · Cited by 13
Metadata
- Authors
- Nylander, K., Vojtesek, B., Nenutil, R., Lindgren, B., Roos, G., Zhanxiang, W., Sjöström, B., Dahlqvist, Å., & Coates, P. J.
- Venue
- The Journal of Pathology
- Publisher
- Wiley
- Published
- 2002-09-13
- Volume
- 198
- Issue
- 4
- Pages
- 417-427
- ISSN
- 0022-3417 (ISSN-L)
- 1096-9896
- OpenAlex
- W2129919885
- Cited by
- 276
- References
- 0
- FWCI
- 6.03
- Type
- journal article
- Language
- en
- Open access
- closed
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